“Like most of us, I had been raised to see illness as something temporary: a stopover on the way to recovery or to death, not a place to live. But weeks, months and then years passed, and I did not get better. My doctors, and even some friends and family members, suggested that I could get better if only I tried harder, relaxed more deeply, thought more positively. I became a lightning rod for others’ fears of disability, dependence and fragility. In a political moment where health care is treated as a luxury and hurricane victims are blamed for their own disasters, an ethic of personal responsibility reigns. But sometimes, sick people just stay sick. And there’s no meditation, medication, positive outlook, exercise or smoothie that can fix it. […] I had once measured my worth by my capacity to produce things and experiences: to be productive at work, share responsibilities at home, “show up” equally in my friendships and rack up achievements. Being sick has been a long, slow detox from capitalist culture and its mandate that we never rest. Slowly, I found a deeper value in relationship beyond reciprocity: an unconditional love and care based in justice, and a belief that all humans deserve relationship, regardless of whether we can offer anything measurable back. In these discoveries, I’ve been led by other sick and disabled people, whose value had always been apparent to me. Amid the brilliant diversity of power wheelchairs, service dogs, canes and ice packs, it’s easy to see that we matter just as we are.”